Canonical Allele Identifier: CA9984001

Gene: TMPRSS15

Linked Data

• ClinVar Variation Id: 1972321
• ClinVar RCV Id: RCV002750287
• dbSNP Id: rs776130106
• ExAC: 21:19653449 A / C
• gnomAD v2: 21-19653449-A-C
• gnomAD v3: 21-18281132-A-C
• gnomAD v4: 21-18281132-A-C
• MyVariant Identifiers: chr21:g.19653449A>C (hg19) ; chr21:g.18281132A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281132A>C , CM000683.2:g.18281132A>C	GRCh38
NC_000021.8:g.19653449A>C , CM000683.1:g.19653449A>C	GRCh37
NC_000021.7:g.18575320A>C	NCBI36
NG_012207.1:g.127522T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2576T>G MANE Select	ENSP00000284885.3:p.Ile859Arg
ENST00000284885.7:c.2576T>G	ENSP00000284885.3:p.Ile859Arg
NM_002772.2:c.2576T>G	NP_002763.2:p.Ile859Arg
XM_011529654.1:c.2711T>G	XP_011527956.1:p.Ile904Arg
XM_011529655.1:c.2711T>G	XP_011527957.1:p.Ile904Arg
XM_011529656.1:c.2711T>G	XP_011527958.1:p.Ile904Arg
XM_011529657.1:c.2666T>G	XP_011527959.1:p.Ile889Arg
XM_011529658.1:c.2630T>G	XP_011527960.1:p.Ile877Arg
XM_011529659.1:c.2621T>G	XP_011527961.1:p.Ile874Arg
XM_011529654.2:c.2711T>G	XP_011527956.1:p.Ile904Arg
XM_011529656.2:c.2711T>G	XP_011527958.1:p.Ile904Arg
XM_011529657.2:c.2666T>G	XP_011527959.1:p.Ile889Arg
XM_011529658.2:c.2630T>G	XP_011527960.1:p.Ile877Arg
NM_002772.3:c.2576T>G MANE Select	NP_002763.3:p.Ile859Arg